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Results: 1 to 20 of 55

1.

Does hip displacement influence health-related quality of life in children with cerebral palsy?

Jung NH, Pereira B, Nehring I, Brix O, Bernius P, Schroeder SA, Kluger GJ, Koehler T, Beyerlein A, Weir S, von Kries R, Narayanan UG, Berweck S, Mall V.

Dev Neurorehabil. 2014 Jul 24:1-6. [Epub ahead of print]

PMID:
25057804
[PubMed - as supplied by publisher]
2.

Current role of rufinamide in the treatment of childhood epilepsy: Literature review and treatment guidelines.

Coppola G, Besag F, Cusmai R, Dulac O, Kluger G, Moavero R, Nabbout R, Nikanorova M, Pisani F, Verrotti A, von Stülpnagel C, Curatolo P.

Eur J Paediatr Neurol. 2014 May 28. pii: S1090-3798(14)00087-7. doi: 10.1016/j.ejpn.2014.05.008. [Epub ahead of print]

PMID:
24929673
[PubMed - as supplied by publisher]
3.

Co-occurring malformations of cortical development and SCN1A gene mutations.

Barba C, Parrini E, Coras R, Galuppi A, Craiu D, Kluger G, Parmeggiani A, Pieper T, Schmitt-Mechelke T, Striano P, Giordano F, Blumcke I, Guerrini R.

Epilepsia. 2014 Jul;55(7):1009-1019. doi: 10.1111/epi.12658. Epub 2014 Jun 5.

PMID:
24902755
[PubMed - as supplied by publisher]
4.

German Translation of the Caregiver Priorities and Child Health Index of Life with Disabilities Questionnaire: Test-Retest Reliability and Correlation with Gross Motor Function in Children with Cerebral Palsy.

Jung NH, Brix O, Bernius P, Schroeder AS, Kluger GJ, Beyerlein A, Weir S, von Kries R, Narayanan UG, Mall V, Berweck S.

Neuropediatrics. 2014 Apr 3. [Epub ahead of print]

PMID:
24700153
[PubMed - as supplied by publisher]
5.

DEPDC5 mutations in genetic focal epilepsies of childhood.

Lal D, Reinthaler EM, Schubert J, Muhle H, Riesch E, Kluger G, Jabbari K, Kawalia A, Bäumel C, Holthausen H, Hahn A, Feucht M, Neophytou B, Haberlandt E, Becker F, Altmüller J, Thiele H, Lemke JR, Lerche H, Nürnberg P, Sander T, Weber Y, Zimprich F, Neubauer BA.

Ann Neurol. 2014 May;75(5):788-92. doi: 10.1002/ana.24127. Epub 2014 Apr 14.

PMID:
24591017
[PubMed - in process]
6.

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.

Suls A, Jaehn JA, Kecskés A, Weber Y, Weckhuysen S, Craiu DC, Siekierska A, Djémié T, Afrikanova T, Gormley P, von Spiczak S, Kluger G, Iliescu CM, Talvik T, Talvik I, Meral C, Caglayan HS, Giraldez BG, Serratosa J, Lemke JR, Hoffman-Zacharska D, Szczepanik E, Barisic N, Komarek V, Hjalgrim H, Møller RS, Linnankivi T, Dimova P, Striano P, Zara F, Marini C, Guerrini R, Depienne C, Baulac S, Kuhlenbäumer G, Crawford AD, Lehesjoki AE, de Witte PA, Palotie A, Lerche H, Esguerra CV, De Jonghe P, Helbig I; EuroEPINOMICS RES Consortium.

Am J Hum Genet. 2013 Nov 7;93(5):967-75. doi: 10.1016/j.ajhg.2013.09.017. Epub 2013 Oct 24.

PMID:
24207121
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.

Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K, Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn JA, Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, Vaher U, Talvik T, Dimova P, Guerrero López R, Serratosa JM, Linnankivi T, Lehesjoki AE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, Kurlemann G, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Sperner J, Becker F, Weber YG, Feucht M, Steinböck H, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J, Harvey RJ, Hoffmann P, Herms S, Altmüller J, Toliat MR, Thiele H, Nürnberg P, Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, von Spiczak S.

Nat Genet. 2013 Sep;45(9):1067-72. doi: 10.1038/ng.2728. Epub 2013 Aug 11.

PMID:
23933819
[PubMed - indexed for MEDLINE]
8.

Advancing the management of childhood epilepsies.

Cross JH, Kluger G, Lagae L.

Eur J Paediatr Neurol. 2013 Jul;17(4):334-47. doi: 10.1016/j.ejpn.2013.02.003. Epub 2013 Apr 1.

PMID:
23558251
[PubMed - indexed for MEDLINE]
9.

Generalized epilepsy in two patients with 5p duplication.

Kluger G, Koehler U, Neuhann TM, Pieper T, Staudt M, von Stülpnagel C.

Neuropediatrics. 2013 Aug;44(4):225-9. doi: 10.1055/s-0033-1333872. Epub 2013 Mar 12.

PMID:
23483447
[PubMed - indexed for MEDLINE]
10.

Lacosamide in pediatric and adult patients: comparison of efficacy and safety.

Verrotti A, Loiacono G, Pizzolorusso A, Parisi P, Bruni O, Luchetti A, Zamponi N, Cappanera S, Grosso S, Kluger G, Janello C, Franzoni E, Elia M, Spalice A, Coppola G, Striano P, Pavone P, Savasta S, Viri M, Romeo A, Aloisi P, Gobbi G, Ferretti A, Cusmai R, Curatolo P.

Seizure. 2013 Apr;22(3):210-6. doi: 10.1016/j.seizure.2012.12.009. Epub 2013 Jan 5.

PMID:
23298605
[PubMed - indexed for MEDLINE]
Free Article
11.

Rufinamide for refractory focal seizures: an open-label, multicenter European study.

Coppola G, Zamponi N, Kluger G, Mueller A, Anna Rita M, Parisi P, Isone C, Santoro E, Curatolo P, Verrotti A.

Seizure. 2013 Jan;22(1):33-6. doi: 10.1016/j.seizure.2012.09.015. Epub 2012 Oct 16.

PMID:
23079159
[PubMed - indexed for MEDLINE]
Free Article
12.

Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations.

Appenzeller S, Helbig I, Stephani U, Häusler M, Kluger G, Bungeroth M, Müller S, Kuhlenbäumer G, van Baalen A.

Dev Med Child Neurol. 2012 Dec;54(12):1144-8. doi: 10.1111/j.1469-8749.2012.04435.x. Epub 2012 Oct 15.

PMID:
23066759
[PubMed - indexed for MEDLINE]
13.

Febrile infection-related epilepsy syndrome without detectable autoantibodies and response to immunotherapy: a case series and discussion of epileptogenesis in FIRES.

van Baalen A, Häusler M, Plecko-Startinig B, Strautmanis J, Vlaho S, Gebhardt B, Rohr A, Abicht A, Kluger G, Stephani U, Probst C, Vincent A, Bien CG.

Neuropediatrics. 2012 Aug;43(4):209-16. doi: 10.1055/s-0032-1323848. Epub 2012 Aug 21.

PMID:
22911482
[PubMed - indexed for MEDLINE]
14.

Bromide in patients with SCN1A-mutations manifesting as Dravet syndrome.

Lotte J, Haberlandt E, Neubauer B, Staudt M, Kluger GJ.

Neuropediatrics. 2012 Feb;43(1):17-21. doi: 10.1055/s-0032-1307454. Epub 2012 Mar 19.

PMID:
22430156
[PubMed - indexed for MEDLINE]
15.

First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome).

von Stülpnagel C, Coppola G, Striano P, Müller A, Staudt M, Kluger G.

Eur J Paediatr Neurol. 2012 Sep;16(5):459-63. doi: 10.1016/j.ejpn.2011.12.012. Epub 2012 Jan 21.

PMID:
22266062
[PubMed - indexed for MEDLINE]
16.

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

Poretti A, Vitiello G, Hennekam RC, Arrigoni F, Bertini E, Borgatti R, Brancati F, D'Arrigo S, Faravelli F, Giordano L, Huisman TA, Iannicelli M, Kluger G, Kyllerman M, Landgren M, Lees MM, Pinelli L, Romaniello R, Scheer I, Schwarz CE, Spiegel R, Tibussek D, Valente EM, Boltshauser E.

Orphanet J Rare Dis. 2012 Jan 11;7:4. doi: 10.1186/1750-1172-7-4.

PMID:
22236771
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Febrile infection-related epilepsy syndrome (FIRES): does duration of anesthesia affect outcome?

Kramer U, Chi CS, Lin KL, Specchio N, Sahin M, Olson H, Kluger G, van Baalen A.

Epilepsia. 2011 Oct;52 Suppl 8:28-30. doi: 10.1111/j.1528-1167.2011.03230.x.

PMID:
21967356
[PubMed - indexed for MEDLINE]
18.

Febrile infection-related epilepsy syndrome (FIRES): pathogenesis, treatment, and outcome: a multicenter study on 77 children.

Kramer U, Chi CS, Lin KL, Specchio N, Sahin M, Olson H, Nabbout R, Kluger G, Lin JJ, van Baalen A.

Epilepsia. 2011 Nov;52(11):1956-65. doi: 10.1111/j.1528-1167.2011.03250.x. Epub 2011 Aug 29.

PMID:
21883180
[PubMed - indexed for MEDLINE]
19.

Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsy.

Ufer M, von Stülpnagel C, Muhle H, Haenisch S, Remmler C, Majed A, Plischke H, Stephani U, Kluger G, Cascorbi I.

Pharmacogenet Genomics. 2011 Oct;21(10):624-30. doi: 10.1097/FPC.0b013e3283498131.

PMID:
21799461
[PubMed - indexed for MEDLINE]
20.

Rufinamide from clinical trials to clinical practice in the United States and Europe.

Resnick T, Arzimanoglou A, Brown LW, Flamini R, Kerr M, Kluger G, Kothare S, Philip S, Harrison M, Narurkar M.

Epileptic Disord. 2011 May;13 Suppl 1:S27-43. doi: 10.1684/epd.2011.0421. Review.

PMID:
21669560
[PubMed - indexed for MEDLINE]

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